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Surface‐Electron Coupling for Efficient Hydrogen Evolution
Author(s) -
Fu Weiwei,
Wang Yanwei,
Hu Jisong,
Zhang Huijuan,
Luo Ping,
Sun Fang,
Ma Xinguo,
Huang Zhengyong,
Li Jian,
Guo Zaiping,
Wang Yu
Publication year - 2019
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201908938
Subject(s) - graphene , density functional theory , chemical physics , adsorption , dissociation (chemistry) , catalysis , hydrogen , materials science , molecule , transition metal , nanotechnology , computational chemistry , chemistry , chemical engineering , organic chemistry , engineering
Maximizing the activity of materials towards the alkaline hydrogen evolution reaction while maintaining their structural stability under realistic working conditions remains an area of active research. Herein, we report the first controllable surface modification of graphene(G)/V 8 C 7 heterostructures by nitrogen. Because the introduced N atoms couple electronically with V atoms, the V sites can reduce the energy barrier for water adsorption and dissociation. Investigation of the multi‐regional synergistic catalysis on N‐modified G/V 8 C 7 by experimental observations and density‐functional‐theory calculations reveals that the increase of electron density on the epitaxial graphene enable it to become favorable for H* adsorption and the subsequent reaction with another H 2 O molecule. This work extends the range of surface‐engineering approaches to optimize the intrinsic properties of materials and could be generalized to the surface modification of other transition‐metal carbides.